Canonical Allele Identifier: PA891845271
Gene: PNP HGNC NCBI

Linked Data

ClinVar Variation Id: 572933
ClinVar RCV Id: RCV000694452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000261.2:p.Thr6Pro
CA7082003
NM_000270.4:c.16A>C